Zobrazeno 1 - 10
of 42
pro vyhledávání: '"GHAZAVI, Ahad"'
Autor:
Gholipoor, Peyman, Saboory, Ehsan, Ghazavi, Ahad, Kiyani, Arezoo, Roshan-Milani, Shiva, Mohammadi, Sedra, Javanmardi, Elmira, Rasmi, Yousef
Publikováno v:
In Epilepsy & Behavior July 2017 72:22-27
Autor:
ABBASI, Ezatolah, GHAZAVI, Ahad, HASSANVAND AMOUZADEH, Masoud, VALIZADEH, Mohammad, AKHAVAN SEPAHI, Mohsen
Publikováno v:
Iranian Journal of Child Neurology
Medium-chain acyl-coA dehydrogenase deficiency (MCADD) is an autosomal recessive disorder of fatty acid β- oxidation, which is inherited in an autosomal recessive manner. The enzyme plays a role in hepatic Ketogenesis, which is a significant source
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::853c168f3ca74ada937dc9e8e929144c
http://europepmc.org/articles/PMC8570626
http://europepmc.org/articles/PMC8570626
Autor:
KARIMZADEH, Parvaneh, TAGHDIRI, Mohammad Mahdi, ABASI, Ezatollah, HASSANVAND AMOUZADEH, Masoud, NAGHAVI, Zhila, GHAZAVI, Ahad, NASEHI, Mohammad Mahdi, ALIPOUR, Abbas
Publikováno v:
Iranian Journal of Child Neurology
Objective Neurometabolic disorder is one of the important groups of diseases that prominently has presentation early infantile period. In this study, we evaluated the result of metabolic screening of the patient with seizure, developmental delay and/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3cc8596845e61970961c7fd041c4f049
http://europepmc.org/articles/PMC5582359
http://europepmc.org/articles/PMC5582359
Autor:
ABBASI, Ezatolah, GHAZAVI, Ahad, HASSANVAND AMOUZADEH, Masoud, VALIZADEH, Mohammad, AKHAVAN SEPAHI, Mohsen
Publikováno v:
Iranian Journal of Child Neurology; Autumn2021, Vol. 15 Issue 4, p89-94, 6p
Autor:
TONEKABONI, Seyed Hassan, JAFARI NAEINI, Sepideh, KHAJEH, Ali, YAGHINI, Omid, GHAZAVI, Ahad, ABDOLLAH GORJI, Fatemeh
Publikováno v:
Iranian Journal of Child Neurology
Objective Although the use of Complementary and Alternative Medicine (CAM) has been evaluated globally, there are few studies in our country on this subject. The purpose of this study was to determine the prevalence, pattern of use, parental sources
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2bfc4dd25833b0843f5bde6439f18655
http://europepmc.org/articles/PMC3943061
http://europepmc.org/articles/PMC3943061
Autor:
ABBASI, Ezatolah, GHAZAVI, Ahad, HASSANVAND AMOUZADEH, Masoud, VALIZADEH, Mohammad, MATINKHAH, Masoud
Publikováno v:
Iranian Journal of Child Neurology; 2020, Vol. 14 Issue 4, p43-53, 11p
Autor:
TONEKABONI, Seyed Hassan, GHAZAVI, Ahad, FAYYAZI, Afshin, KHAJEH, Ali, TAGHDIRI, Mohammad Mahdi, ABDOLLAH GORJI, Fatemeh, AZARGHASHB, Eznollah
Publikováno v:
Iranian Journal of Child Neurology
Objective Headache is a common disabling neurological disorder and migraine comprises more than half the causes of recurrent headaches in children. Despite extended prevalence of this type of headache there is lack of evidence about best drug treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95dc110163a4315d4e3ed481e89e45c8
http://europepmc.org/articles/PMC3943076
http://europepmc.org/articles/PMC3943076
This study was carried out to determine the frequency of the VNTR-polymorphisms at the PAH gene in the Iranian Azeri Turkish patients with phenylketonuria (PKU) and normal controls.The VNTR-polymorphisms were determined by PCR in 43 PKU patients as w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::23f41200f016de4174108b1be876fc6f
https://europepmc.org/articles/PMC5394437/
https://europepmc.org/articles/PMC5394437/
Akademický článek
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Publikováno v:
Iranian Journal of Child Neurology; Winter2016, Vol. 10 Issue 1, p9-13, 5p, 1 Chart